Clinical Research Coordinator — Hybrid/Remote for Complex Studies

University Of Michigan; Ann Arbor (MI); Hybrid; USD 60,000 - 85,000; Full time

Job summary

Michigan Medicine seeks a Clinical Research Coordinator to support multiple studies, with independence across tasks and quality-focused execution. The role requires expertise across consent, data collection, regulatory affairs, and study operations within a hybrid work setting.

The position involves patient interaction, regulatory coordination, budgeting support, and IRB submissions, with supervision by experienced investigators.

Qualifications

• Bachelor's degree in Health Science or an equivalent combination of related education and experience is necessary.
• Certification through ACRP as CRC or SOCRA as CCRP (or equivalent) and eligibility to register or take the exam within six months.
• Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
• Minimum 1 year of directly related clinical research experience; advanced degree in health-related areas or 3 years of human-subject experience may satisfy qualifications.

Responsibilities

• Interact with research participants via telephone, telehealth or in-person.
• Coordinate regulatory documentation to comply with FDA/Hospital policies.
• Schedule procedures and assist with consent processes.
• Screen, recruit, enroll and follow subjects per study protocol.
• Maintain data collection and develop CRFs or data tools.
• Assist in developing and implementing research studies and protocols.
• Ensure safety reporting per protocol and HRPP standards.
• May assist PI with budget preparation and billing activities.
• Prepare IRB submissions and amendments; coordinate with research teams.

Skills

Clinical research experience

Certification (ACRP/SOCRA)

Communication skills

Independent worker

Education

Bachelor's degree in Health Science or equivalent

Associate degree in Health Science or equivalent

Tools

Electronic data capture systems

Job description

Michigan Medicine seeks a Clinical Research Coordinator to support multiple studies, with independence across tasks and quality-focused execution. The role requires expertise across consent, data collection, regulatory affairs, and study operations within a hybrid work setting.

The position involves patient interaction, regulatory coordination, budgeting support, and IRB submissions, with supervision by experienced investigators.